The Recall Desk

State

Northern Mariana Islands product recalls

73,827 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total
23
Critical
0
Severe
18
Most recent
2026-09-23

Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55351–55375 of 73850

  • HighFDA (Devices)·Z-1052-2015·2015-02-11

    Zimmer Recalls Persona Tibial Articular Surface Provisional Shims Due to Cleaning Defect

    Zimmer, Inc. is recalling Persona Tibial Articular Surface Provisional Shims because repeated sonic cleaning can break the ball bearing retention feature, potentially leaving parts in the surgical wound.

    Product
    Persona (TASP) Tibial Articular Surface Provisional Shim, all sizes and Lots Catalog Number: 42-5279-002-00 thru 42-5279-009-04. Product Usage: The Persona TASPs are sterilizable instruments Intended for multiple uses. The TASP components are used to aid the surgeon in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1041-2015·2015-02-11

    Roche Cobas b 221 Blood Gas Analyzer Recalled for Measurement Bias

    Roche Diagnostics is recalling 103 Cobas b 221 analyzers because bacterial contamination causes inaccurate glucose and lactate readings.

    Product
    Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0974-2015·2015-02-11

    Zilks Hummus with Real Bacon Recalled for Potential Undeclared Peanuts

    Zilks Foods is recalling 3,808 cups of hummus with real bacon due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS HUMMUS with REAL BACON GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1053-2015·2015-02-11

    CareFusion Recalls SmartSite Infusion Sets Due to Disconnection and Leakage

    CareFusion is recalling 7,440 SmartSite Low Sorbing Infusion Sets due to disconnection and leakage issues.

    Product
    SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein. The set is comprised of components commonly found on intravascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1058-2015·2015-02-11

    Puritan Bennett 980 Ventilator Recalled for Occasional GUI Resets

    Covidien is voluntarily recalling 418 Puritan Bennett 980 ventilators due to occasional graphical user interface resets lasting approximately 30 seconds.

    Product
    Puritan Bennett 980 Ventilator System, Model No. PB980 Ventilator (980xxxxxxxx), The Puritan BennettTM 980 Ventilator System is designed for use on Neonatal (NICU) through Adult patient populations who require respiratory support or mechanical ventilation and weigh a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0383-2015·2015-02-11

    Taro Recalls Children's Loratadine Syrup Due to Blue Plastic Presence

    Taro Pharmaceuticals is recalling 36,684 bottles of Children's Loratadine Syrup because blue plastic was found floating in the liquid.

    Product
    Children's Loratadine Syrup (Loratadine Oral Solution) 5 mg/5 mL, Antihistamine, Grape Flavored Syrup, 24 Hour Non-Drowsy Allergy Relief Sugar Free, 4 FL OZ (120 mL) Bottles, Distributed by: Taro Pharmaceuticals U.S.A., Inc. Hawthorne, NY 10532. NDC: 51672-2092-8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1048-2015·2015-02-11

    Intuitive Surgical Recalls da Vinci Si Wall Charts for Sterilization Inconsistency

    Intuitive Surgical is recalling 1,034 da Vinci Si Wall Charts because they contained incorrect sterilization dry time information inconsistent with the User Manual.

    Product
    da Vinci Si Surgical System, IS3000; - Wall chart for EndoWrist Stapler 45 System. Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1057-2015·2015-02-11

    Medtronic Recalls KYPHON EXPRESS Osteo Introducer System Due to Labeling Error

    Medtronic is recalling 239 units of the KYPHON EXPRESS Osteo Introducer System because the packaging may contain the wrong instrument tips.

    Product
    KYPHON EXPRESS, Osteo Introducer System, Diamond and Bevel, Size 2, REF T34A, QTY: 1EA, Rx only, STERILE R. For use with spinal fixation devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1043-2015·2015-02-11

    Stryker Recalls Trident PSL Hip Shells Missing Dome Hole Plugs

    Stryker Howmedica Osteonics is recalling seven units of Trident PSL HA Solid Back 50 mm hip shells because the dome hole plugs were missing from the packages.

    Product
    Trident PSL HA Solid Back 50 mm Includes Dome Hole Plug Ref 540-11-50E Intended for cementless application in a total hip arthroplasty procedure. This system is a two piece ( a shell and a liner) design that is assembled during surgery. The shell is press-fit into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0942-2015·2015-02-11

    Gemini Foods Recalls Dried Bean Curd Due to Dimethyl Yellow Contamination

    Gemini Foods is recalling dried bean curd products because they may be contaminated with dimethyl yellow. The recall covers 3,360 units distributed nationwide.

    Product
    Dried Bean Curd Anka Flavor 24x150g, Item No. 8535
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15T004000·2015-02-10

    Tireco Recalls Milestar Tires Due to Sidewall Cracking Risk

    Tireco is recalling specific Milestar tires manufactured in 2014 because they may crack in the lower sidewall, increasing the risk of sudden failure and crashes.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V081000·2015-02-10

    Toyota Recalls 2014 FJ Cruiser for Steering Shaft Weld Defect

    Toyota is recalling 2014 FJ Cruisers due to a potential inadequate weld on the intermediate steering shaft, which could lead to loss of steering control.

    Product
    TOYOTA — TOYOTA FJ CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V082000·2015-02-10

    Mercedes-Benz Recalls 2015 Sprinter 2500 and 3500 for Door Defect

    Mercedes-Benz is recalling 2015 Sprinter 2500 and 3500 vans because an incorrectly installed door component may make doors harder to open after a severe frontal crash.

    Product
    MERCEDES BENZ — MERCEDES BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15076·2015-02-10

    Marin Recalls 2014 MBX 50 and Tiny Trail Children's Bicycles

    Marin Mountain Bikes is recalling 2014 MBX 50 and Tiny Trail children's bicycles because handlebars can loosen or separate, posing a crash and injury risk.

    Product
    2014 Marin MBX 50 and Tiny Trail Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V080000·2015-02-10

    Forest River Recalls 2014 Rockwood and Flagstaff RVs for Fire Risk

    Forest River is recalling 726 model year 2014 Rockwood and Flagstaff recreational vehicles equipped with the Chill Chaser option due to a fire risk from loose wiring or foam insulation contacting the heating element.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V079000·2015-02-09

    Nova Bus Recalls 2009 LFS Transit Buses for Brake Hose Fitting Defect

    Nova Bus is recalling 2009 LFS transit buses because damaged brake hose crimping rings may fail, affecting braking performance and increasing crash risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V077000·2015-02-09

    Nova Bus Recalls 2007-2009 LFS Transit Buses for Fire Risk

    Nova Bus is recalling 2007-2009 LFS transit buses because a battery cable may short to ground, increasing the risk of a fire.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V076000·2015-02-09

    Nova Bus Recalls 2008 LFS Transit Buses for Emergency Exit Defect

    Nova Bus is recalling 2008 LFS transit buses because surrounding material may interfere with opening emergency exit windows, increasing injury risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide